JP5971834B2 - 耐フォギング性を有する帯電防止剤を含有してなるポリオレフィン系樹脂組成物 - Google Patents
耐フォギング性を有する帯電防止剤を含有してなるポリオレフィン系樹脂組成物 Download PDFInfo
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- JP5971834B2 JP5971834B2 JP2010085043A JP2010085043A JP5971834B2 JP 5971834 B2 JP5971834 B2 JP 5971834B2 JP 2010085043 A JP2010085043 A JP 2010085043A JP 2010085043 A JP2010085043 A JP 2010085043A JP 5971834 B2 JP5971834 B2 JP 5971834B2
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- Prior art keywords
- polyolefin resin
- resin composition
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- polyolefin
- antistatic agent
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- 125000000217 alkyl group Chemical group 0.000 claims description 8
- 125000004432 carbon atom Chemical group C* 0.000 claims description 7
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- 238000012360 testing method Methods 0.000 description 27
- 238000005259 measurement Methods 0.000 description 23
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- 238000005033 Fourier transform infrared spectroscopy Methods 0.000 description 16
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- 238000005160 1H NMR spectroscopy Methods 0.000 description 10
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- 125000003438 dodecyl group Chemical group [H]C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])* 0.000 description 2
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- VTHJTEIRLNZDEV-UHFFFAOYSA-L magnesium dihydroxide Chemical compound [OH-].[OH-].[Mg+2] VTHJTEIRLNZDEV-UHFFFAOYSA-L 0.000 description 2
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- YODZTKMDCQEPHD-UHFFFAOYSA-N thiodiglycol Chemical compound OCCSCCO YODZTKMDCQEPHD-UHFFFAOYSA-N 0.000 description 1
- STCOOQWBFONSKY-UHFFFAOYSA-N tributyl phosphate Chemical compound CCCCOP(=O)(OCCCC)OCCCC STCOOQWBFONSKY-UHFFFAOYSA-N 0.000 description 1
- 125000002469 tricosyl group Chemical group [H]C([*])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])C([H])([H])[H] 0.000 description 1
- DQWPFSLDHJDLRL-UHFFFAOYSA-N triethyl phosphate Chemical compound CCOP(=O)(OCC)OCC DQWPFSLDHJDLRL-UHFFFAOYSA-N 0.000 description 1
- WVLBCYQITXONBZ-UHFFFAOYSA-N trimethyl phosphate Chemical compound COP(=O)(OC)OC WVLBCYQITXONBZ-UHFFFAOYSA-N 0.000 description 1
- XZZNDPSIHUTMOC-UHFFFAOYSA-N triphenyl phosphate Chemical compound C=1C=CC=CC=1OP(OC=1C=CC=CC=1)(=O)OC1=CC=CC=C1 XZZNDPSIHUTMOC-UHFFFAOYSA-N 0.000 description 1
- KOWVWXQNQNCRRS-UHFFFAOYSA-N tris(2,4-dimethylphenyl) phosphate Chemical compound CC1=CC(C)=CC=C1OP(=O)(OC=1C(=CC(C)=CC=1)C)OC1=CC=C(C)C=C1C KOWVWXQNQNCRRS-UHFFFAOYSA-N 0.000 description 1
- WTLBZVNBAKMVDP-UHFFFAOYSA-N tris(2-butoxyethyl) phosphate Chemical compound CCCCOCCOP(=O)(OCCOCCCC)OCCOCCCC WTLBZVNBAKMVDP-UHFFFAOYSA-N 0.000 description 1
- LIPMRGQQBZJCTM-UHFFFAOYSA-N tris(2-propan-2-ylphenyl) phosphate Chemical compound CC(C)C1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C(C)C)OC1=CC=CC=C1C(C)C LIPMRGQQBZJCTM-UHFFFAOYSA-N 0.000 description 1
- SPUXJWDKFVXXBI-UHFFFAOYSA-N tris(2-tert-butylphenyl) phosphate Chemical compound CC(C)(C)C1=CC=CC=C1OP(=O)(OC=1C(=CC=CC=1)C(C)(C)C)OC1=CC=CC=C1C(C)(C)C SPUXJWDKFVXXBI-UHFFFAOYSA-N 0.000 description 1
- QQBLOZGVRHAYGT-UHFFFAOYSA-N tris-decyl phosphite Chemical compound CCCCCCCCCCOP(OCCCCCCCCCC)OCCCCCCCCCC QQBLOZGVRHAYGT-UHFFFAOYSA-N 0.000 description 1
- KPGXUAIFQMJJFB-UHFFFAOYSA-H tungsten hexachloride Chemical compound Cl[W](Cl)(Cl)(Cl)(Cl)Cl KPGXUAIFQMJJFB-UHFFFAOYSA-H 0.000 description 1
- 229940088594 vitamin Drugs 0.000 description 1
- 229930003231 vitamin Natural products 0.000 description 1
- 239000002699 waste material Substances 0.000 description 1
- XLYOFNOQVPJJNP-UHFFFAOYSA-N water Substances O XLYOFNOQVPJJNP-UHFFFAOYSA-N 0.000 description 1
- 229940045860 white wax Drugs 0.000 description 1
- 239000002023 wood Substances 0.000 description 1
- UGZADUVQMDAIAO-UHFFFAOYSA-L zinc hydroxide Chemical compound [OH-].[OH-].[Zn+2] UGZADUVQMDAIAO-UHFFFAOYSA-L 0.000 description 1
- 229910021511 zinc hydroxide Inorganic materials 0.000 description 1
- 229940007718 zinc hydroxide Drugs 0.000 description 1
- 239000004711 α-olefin Substances 0.000 description 1
Description
即ち本発明は、ポリオレフィン系樹脂中に、下記一般式(I)〜(III)で表されるジウレタン構造を有する化合物からなる群の中から選択される耐フォギング性を有する帯電防止剤を含有してなることを特徴とするポリオレフィン系樹脂組成物である。
但し、上式中のR1及びR2は、同一でも異なっていてもよい炭素原子数が12以上のアルキル基であり、n及びmは、同一でも異なっていてもよい2〜30の数である。
更に本発明のポリオレフィン系樹脂組成物においては、前記帯電防止剤の含有量が、ポリオレフィン系樹脂100質量部に対し、0.01〜20質量部であることが好ましく、0.05〜15質量部であることが更に好ましく、1〜10質量部であることが最も好ましい。また、前記ポリオレフィン系樹脂は、ポリプロピレン系樹脂又はポリエチレン系樹脂であることが好ましい。
但し、上式中のR1及びR2は、同一でも異なっていてもよい炭素原子数が12以上のアルキル基であり、n及びmは、同一でも異なっていてもよい2〜30の数である。
上記の一般式(IV)で表されるジイソシアネート化合物は、一般式(I)の場合はm−キシリレンジイソシアネート、一般式(II)の場合は2,4−トリレンジイソシアネートであり、一般式(III)の場合はジシクロヘキシルメタン4,4−ジイソシアネートである。
また、前記一般式(V)中のRは、一般式(I)〜(III)中のR1又はR2に対応するアルキル基、qは、前記一般式(I)〜(III)中のn又はmに対応する2〜30の数である。
5−ジ第三ブチル−4−ヒドロキシベンジル)−2,4,6−トリメチルベンゼン、2−第三ブチル−4−メチル−6−(2−アクリロイルオキシ−3−第三ブチル−5−メチルベンジル)フェノール、ステアリル(3,5−ジ第三ブチル−4−ヒドロキシフェニル)プロピオネート、テトラキス〔3−(3,5−ジ第三ブチル−4−ヒドロキシフェニル)プロピオン酸メチル〕メタン、チオジエチレングリコールビス〔(3,5−ジ第三ブチル−4−ヒドロキシフェニル)プロピオネート〕、1,6−ヘキサメチレンビス〔(3,5−ジ第三ブチル−4−ヒドロキシフェニル)プロピオネート〕、ビス〔3,3−ビス(4−ヒドロキシ−3−第三ブチルフェニル)ブチリックアシッド〕グリコールエステル、ビス〔2−第三ブチル−4−メチル−6−(2−ヒドロキシ−3−第三ブチル−5−メチルベンジル)フェニル〕テレフタレート、1,3,5−トリス〔(3,5−ジ第三ブチル−4−ヒドロキシフェニル)プロピオニルオキシエチル〕イソシアヌレート、3,9−ビス〔1,1−ジメチル−2−{(3−第三ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオニルオキシ}エチル〕−2,4,8,10−テトラオキサスピロ〔5,5〕ウンデカン、トリエチレングリコールビス〔(3−第三ブチル−4−ヒドロキシ−5−メチルフェニル)プロピオネート〕等が挙げられる。これらのフェノール系酸化防止剤の添加量は、ポリオレフィン系樹脂100質量部に対して、0.001〜10質量部であることが好ましく、特に0.05〜5質量部であることが好ましい。
上記非イオン性界面活性剤としては、例えば、高級アルコールエチレンオキシド付加物、脂肪酸エチレンオキシド付加物、高級アルキルアミンエチレンオキシド付加物、ポリプロピレングリコールエチレンオキシド付加物等のポリエチレングリコール型非イオン性界面活性剤;ポリエチレンオキシド、グリセリンの脂肪酸エステル、ペンタエリスリットの脂肪酸エステル、ソルビット又はソルビタンの脂肪酸エステル、多価アルコールのアルキルエーテル、アルカノールアミンの脂肪族アミド等の、多価アルコール型非イオン性界面活性剤が挙げられる。
200mlの三つ口フラスコに、ポリオキシエチレンモノステアリルエーテル(HO−(CH2CH2O)15−C18H37)76g(0.083モル)とm−キシリレンジイソシアネート7.8g(0.0415モル)を、窒素雰囲気下、120℃で4時間反応させた。FT−IRによりイソシアネート基のピーク(約2250cm−1)の消失を確認した後、60℃まで冷却し、次いでアルミホイル製のバット上に回収して白色個体の試験化合物−1を得た(収率95%)。
FT−IR測定結果(cm−1): 3340、2854、1720、1110
1H−NMR測定結果(CDCl3溶媒)
(ケミカルシフト(ppm);多重度;プロトン数):
(7.3-7.2;m;4H)、(4.35;dd;2H)、(4.25;m;2H)、(3.72;dd;4H)、(3.7-3.5;m;112H)、(3.44;t;4H)、(1.59;t;4H)、(1.25;m;58H)、(0.88;t;6H)
200mlの三つ口フラスコに、ポリオキシエチレンモノステアリルエーテル(HO−(CH2CH2O)15−C18H37)65g(0.071モル)とイソホロンジイソシアネート7.9g(0.0355モル)を、窒素雰囲気下、120℃で4時間反応させた。FT−IRによりイソシアネート基のピーク(約2250cm−1)の消失を確認した後、60℃まで冷却し、次いでアルミホイル製のバット上に回収して白色個体の試験化合物−2を得た(収率97%)。
FT−IR測定結果(cm−1): 3340、2854、1720、1110
1H−NMR測定結果(CDCl3溶媒)
(ケミカルシフト(ppm);多重度;プロトン数):
(4.2;m;4H)、(3.8−3.6;m;112H)、(3.57;t;4H)、(3.53;m;1H)、(3.44;t;4H)、(2.92;d;2H)、(1.81;s;2H)、(1.70;m;2H)、(1.57;m;4H)、(1.25;m;60H)、(1.06;s;6H)、(0.92;s;3H)、(0.88;t;6H)
200mlの三つ口フラスコにポリオキシエチレンモノステアリルエーテル(HO−(CH2CH2O)15−C18H37)65g(0.071mol)と2,4−トリレンジイソシアネート6.2g(0.0355mol)を、窒素雰囲気下、120℃で4時間反応させた。FT−IRによりイソシアネート基のピーク(約2250cm−1)の消失を確認した後、60℃まで冷却してサンプル瓶に回収し、白色状ワックスの試験化合物−3を得た(収率95%)。
FT−IR測定結果(cm−1):3300、2860、1730、1110
1H−NMR測定結果(CDCl3溶媒)
(ケミカルシフト(ppm);多重度;プロトン数):
(7.83;m;1H)、(7.21;m;1H)、(7.07;d;1H)、(4.30;m;4H)、(3.74;m;4H)、(3.7−3.5;m;112H)、(3.44;t;4H)、(2.19;s;3H)、(1.59;t;4H)、(1.25;m;60H)、(0.88;t;6H)
200mlの三つ口フラスコにポリオキシエチレンモノステアリルエーテル(HO−(CH2CH2O)15−C18H37)65g(0.071mol)とジシクロヘキシルメタン4,4'-ジイソシアナート10.3g(0.0355mol)を、窒素雰囲気下、120℃で4時間反応させた。FT−IRによりイソシアネート基のピーク(約2250cm−1)の消失を確認した後、60℃まで冷却してアルミホイル製のバット上に回収し、白色固体の試験化合物−4を得た(収率96%)。
FT−IR測定結果(cm−1):3340、2854、1720、1110
1H−NMR測定結果(CDCl3溶媒)
(ケミカルシフト(ppm);多重度;プロトン数):
(4.20;m;4H)、(3.7−3.55;m;112H)、(3.58;m;4H)、(3.44;t;4H)、(1.98;m;2H)、(1.78;m;2H)、(1.71;m;2H)、(1.65;m;2H)、(1.55;m;8H)、(1.25;m;60H)、(1.07;m;6H)、(0.97;m;2H)、(0.88;t;6H)
200mlの三つ口フラスコにポリオキシエチレンモノステアリルエーテル(HO−(CH2CH2O)20−C18H37)76g(0.066mol)とm−キシリレンジイソシアネート6.3g(0.033mol)を、窒素雰囲気下、120℃で4時間反応させた。FT−IRによりイソシアネート基のピーク(約2250cm−1)の消失を確認した後、60℃まで冷却してアルミホイル製のバット上に回収し、白色固体の試験化合物−5を得た(収率95%)。
FT−IR測定結果(cm−1):3340、2854、1720、1110
1H−NMR測定結果(CDCl3溶媒)
(ケミカルシフト(ppm);多重度;プロトン数):
(7.3―7.2;m;4H)、(4.35;dd;2H)、(4.25;m;2H)、(3.72;dd;4H)、(3.7−3.5;m;156H)、(3.44;t;4H)、(1.59;t;4H)、(1.25;m;60H)、(0.88;t;6H)
下記の条件で、試験化合物-1を用いて試験片を作製し、下記の条件で性能評価を行った結果を、表1及び2に示した。また比較品−1として、グリセリンモノステアレート(商品名リケマールS−100 理研ビタミン(株)製)、比較品−2としてポリエーテルエステル型帯電防止剤(三洋化成(株)製:商品名ペレスタット300)を用いて同様に評価した。結果を合わせて表1及び2に示す。
表1及び2に記載した配合量に基づいてブレンドしたポリプロピレン樹脂組成物を、(株)池貝製2軸押出機(PCM30,60mesh入り)を用い、200℃、6kg/時間で造粒し、得られたペレットを200℃でプレス成形して試験片(100mm×100mm×1mm)を得た。
得られた試験片について、成形加工後直ちに25℃で湿度60%の条件下に保存し、成形加工の2日後、1週間後及び2週間保存後に、同じ雰囲気下で、アドバンテスト社製のR8340抵抗計を用いて、印加電圧100V、印加時間1分の条件で、表面固有抵抗値(Ω/□)を測定した。測定は5点について行った。その平均値を表1及び2に示す。
上記で得られた試験片の表面を、ウエスで50回乾拭きし、25℃で湿度60%の条件下に2時間保存した後、同雰囲気下にて、アドバンテスト社製のR8340抵抗計を用いて、印加電圧100V、印加時間1分の条件で、表面固有抵抗値(Ω/□)を測定した。測定は5点について行った。その平均値を表1及び2に示す。
上記で得られたペレットをサンプル瓶に入れて上部をガラス板で蓋をし、120℃のオイルバス中で1時間加熱した。なお、ガラス板は氷水で冷却した。1時間後にガラス板のヘイズ値を測定し、ペレットからの気散の程度を比較した。結果を表1及び2に示す。
試験化合物-1の代わりに試験化合物-3〜5を用いたこと以外は、実施例1と同様の条件で各試験片を作製し、性能評価を行った。結果を表3に示す。
<試験片作製条件>
表4に記載した配合量に基づいてブレンドしたポリプロピレン樹脂組成物を、(株)池貝製2軸押出機(PCM30,60mesh入り)を用い、200℃、6kg/時間で造粒し、得られたペレットを200℃で射出成形して試験片(100mm×100mm×1mm)を得た。
得られた各試験片について、実施例1と同様にして性能評価を行った。結果を表4に示す。
これに対し、本発明のポリオレフィン系樹脂組成物は、帯電防止性が優れていること、及び、このポリオレフィン系樹脂組成物を使用する樹脂成形体の帯電防止性能の持続性が良好であることも確認された。
Claims (7)
- 前記n及びmが5〜25の数である、請求項1に記載されたポリオレフィン系樹脂組成物。
- 前記n及びmが10〜20の数である、請求項2に記載されたポリオレフィン系樹脂組成物。
- 前記ポリオレフィン系樹脂が、ポリプロピレン系樹脂又はポリエチレン系樹脂である、請求項1〜3の何れかに記載されたポリオレフィン系樹脂組成物。
- 前記帯電防止剤の含有量が前記ポリオレフィン系樹脂100質量部に対し0.01〜20質量部である、請求項1〜4の何れかに記載されたポリオレフィン系樹脂組成物。
- 前記帯電防止剤の含有量が、前記ポリオレフィン系樹脂100質量部に対し0.05〜15質量部である、請求項5に記載されたポリオレフィン系樹脂組成物。
- 前記帯電防止剤が、前記一般式(III)で表される化合物である、請求項1〜6の何れかに記載されたポリオレフィン系樹脂組成物。
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